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Glucocerebrosidase Processing in Normal Fibroblasts and in Fibroblasts from Patients with Type I, Type II, and Type III Gaucher Disease

✍ Scribed by Ernest Beutler and Wanda Kuhl


Book ID
123633501
Publisher
National Academy of Sciences
Year
1986
Tongue
English
Weight
738 KB
Volume
83
Category
Article
ISSN
0027-8424

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## Communicated by Mark Paalman Gaucher disease, the most common lysosomal storage disorder, results from the inherited deficiency of the enzyme glucocerebrosidase. Three clinical types are recognized: type 1, nonneuronopathic; type 2, acute neuronopathic; and type 3, subacute neuronopathic. Type 2